chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5152779535152779536AT14GENIChomozygous55929465
5152779590152779591GA16GENIChomozygous55799275
5152779926152779927AG14GENIChomozygous55799277
5152780705152780706TC9GENIChomozygous55929467
5152781066152781067AT17GENIChomozygous55799278
5152782767152782768TA16GENIChomozygous55929469
5152782820152782821GA6GENIChomozygous56461258
5152782822152782823AG10GENIChomozygous55799282
5152782979152782980TTC2GENIChomozygous55799283
5152783347152783348TG7GENIChomozygous55929471
5152783352152783353AC7GENIChomozygous55929473
5152784507152784508CT8GENIChomozygous55929479
5152784676152784677GA15GENIChomozygous55929481
5152784858152784859AG12GENIChomozygous55929483
5152784884152784885AC14GENIChomozygous55799294
5152784914152784915GA9GENIChomozygous55929485
5152784918152784919AG8GENIChomozygous55799295
5152785021152785022TG13GENIChomozygous55929487
5152785518152785520TT--17GENIChomozygous55929489
5152785575152785576CT20GENIChomozygous55929491
5152785687152785688AAAAGATCACCAAACAGGG23GENIChomozygous55799296
5152786156152786157CT7GENIChomozygous55799298
5152787238152787239TA50GENIChomozygous55799301
5152787322152787323TTCACA8GENICheterozygous56461259
5152787331152787332CCAT8GENICpossibly homozygous56461260
5152787360152787361GA10GENICheterozygous55799302
5152787394152787395TC21GENIChomozygous55799305